Increase in blood derived mitochondrial DNA copy number in strabismus patients.

Background: Abnormalities in mitochondrial energy homeostasis can lead to various disorders, including ocular motility aberrations. Previous studies have suggested the involvement of mitochondrial aberrations in strabismus etiology. We compared the blood-derived mitochondrial DNA (mtDNA) copy number from comitant strabismus patients with that from age-matched controls, and also compared expression of mitochondrial biogenesis genes in a separate set of extraocular muscle samples from strabismic and control subjects.

Prevalence of strabismus in Pakistan: a systematic review and meta-analysis.

: Strabismus is an ocular condition characterized by misalignment of the visual axis. The global prevalence of strabismus is about 2-3%, which varies between different countries and ethnicities. The aim of this study was to conduct a meta-analysis of studies, which had previously reported the prevalence of strabismus in Pakistan, in order to obtain the overall prevalence of strabismus in the country.

Exploring WNT2 polymorphisms in comitant strabismus: A genetic association study.

Background: Strabismus is a complex oculomotor condition characterized by a misalignment of the visual axis. The genetics of strabismus are poorly defined although a few candidate genes have been identified, among which is the WNT2 gene. Our study was designed to assess the association of single nucleotide polymorphisms (SNPs) of WNT2 in Pakistani strabismus patients.

Association of polymorphisms with exotropia in a Pakistani cohort.

Purpose: Strabismus (STBMS) is a multifactorial ocular disorder in children that leads to misalignment of the eyes. Insulin-like growth factor 1 () has been shown to be involved in the development of extraocular muscles and myopia; however, data are limited on the genetic associations of with STBMS in Pakistan.

Methods: Two hundred seventy-four STBMS cases and 272 unaffected controls were recruited, and their DNA was extracted.